Evidence map›Paper›PMID 20717741›Full record

ReviewImmunologic research2010

Prospects of a novel vaccination strategy for human gamma-herpesviruses.

Ting-Ting Wu, Marcia A Blackman, Ren Sun

Abstract readReview
In one paragraph

Review in Immunologic research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Immune Control ofViral immunology · 2020
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Ting-Ting WuDepartment of Molecular and Medical Pharmacology, School of Medicine, University of California at Los Angeles, CA 90095, USA. twu@mednet.ucla.edu
Marcia A Blackman
Ren Sun
University of California, Los Angeles · USTrudeau Institute · US

Funding

ORF36 Viral Kinase as a Transcriptional Regulator of KSHVP01DE019085 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SUN, REN · 2008 to 2012
$6.4M
T CELL IMMUNITY TO MHV 68, A MURINE GAMMA HERPEVIRUSR01AI042927 · NIAID · TRUDEAU INSTITUTE, INC. · PI BLACKMAN, MARCIA A · 1998 to 2008
$2.5M
Research Training in Immunology and Infectious DiseasesT32AI049823 · NIAID · TRUDEAU INSTITUTE, INC. · PI COOPER, ANDREA M · 2001 to 2015
$2.1M
Role of Interleukin-6 in Gammaherpesvirus replicationR01DE015752 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SUN, REN · 2003 to 2007
$1.6M
Immunogenicity and efficacy of genetically engineered gamma-herpesvirus vaccinesRC2CA148250 · NCI · TRUDEAU INSTITUTE, INC. · PI BLACKMAN, MARCIA A, SUN, REN · 2009 to 2010
$1000k
POLYADENYLATED NUCLEAR RNA OF HUMAN HERPESVIRUS-8R01CA083525 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SUN, REN · 1999 to 2001
$472k
Genetic Analysis of Interactions Between Oral Innate Immunity and a HerpesvirusR21DE018337 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WU, TING-TING · 2007 to 2008
$421k
CD* T cell responses to gamma-herpesviral infectionF32AI084327 · NIAID · TRUDEAU INSTITUTE, INC. · PI FREEMAN, MICHAEL L · 2009 to 2010
$98k
NCI NIH HHS CA148250NCI NIH HHS RC2 CA148250NIAID NIH HHS AI42927NIAID NIH HHS F32 AI084327NIAID NIH HHS F32AI084327NIAID NIH HHS R01 AI042927NIAID NIH HHS T32 AI049823NIAID NIH HHS T32 AI49823NIDCR NIH HHS DE15752NIDCR NIH HHS DE18337NIDCR NIH HHS DE19085NIDCR NIH HHS P01 DE019085NIDCR NIH HHS R01 DE015752NIDCR NIH HHS R21 DE018337
6 · The paper itself

Abstract

Due to the oncogenic potential associated with persistent infection of human gamma-herpesviruses, including Epstein-Barr virus (EBV or HHV-4) and Kaposi's sarcoma-associated herpesvirus (KSHV or HHV-8), vaccine development has focused on subunit vaccines. However, the results using an animal model of mouse infection with a related rodent virus, murine gamma-herpesvirus 68 (MHV-68, γHV-68, or MuHV-4), have shown that the only effective vaccination strategy is based on live attenuated viruses, including viruses engineered to be incapable of establishing persistence. Vaccination with a virus lacking persistence would eliminate many potential complications. Progress in understanding persistent infections of EBV and KSHV raises the possibility of engineering a live attenuated virus without persistence. Therefore, we should keep the option open for developing a live EBV or KSHV vaccine.

Indexed as

Herpesvirus VaccinesVirus LatencyAnimalsCell Transformation, NeoplasticCell Transformation, ViralDisease Models, AnimalGammaherpesvirinaeHerpesviridae InfectionsHumansImmune EvasionMiceTumor Virus InfectionsVaccinationVaccines, AttenuatedVirus ReplicationHerpesvirus VaccinesVaccines, Attenuated

Identifiers

PMID20717741
PMCPMC3931126
OpenAlexW2026577388

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.